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Researchers say the design of AAVs has generated gene therapy delivery vectors that are better at crossing the blood-brain barrier to treat CNS diseases.

United statesNick paul taylorYulia grishchukBrigham departmentScience advisory boardNature biomedical engineeringBrave bioGenomic medicineMassachusetts general hospitalGene therapyGene therapiesCentral nervous systemAdeno associated virusesBlood brain barrierIral capsidsCns diseases